Congenital Hepatic Arteriovenous Malformation Presenting with Severe Persistent Pulmonary Hypertension

被引:5
|
作者
Thatrimontrichai, Anucha [1 ]
Chanvitan, Prasin [1 ]
Janjindamai, Waricha [1 ]
Dissaneevate, Supaporn [1 ]
Kritsaneepaiboon, Supika [2 ]
Hongsakul, Keerati [2 ]
机构
[1] Prince Songkla Univ, Fac Med, Dept Pediat, Div Neonatol, Hat Yai 90110, Songkhla, Thailand
[2] Prince Songkla Univ, Fac Med, Dept Radiol, Hat Yai 90110, Songkhla, Thailand
来源
INDIAN JOURNAL OF PEDIATRICS | 2012年 / 79卷 / 05期
关键词
Arteriovenous malformation; Embolization; Hepatic; Neonate; Pulmonary hypertension; Respiratory distress;
D O I
10.1007/s12098-011-0512-z
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Congenital hepatic arteriovenous malformation is a rarely seen vascular malformation with persistent pulmonary hypertension in neonates. The authors report a full-term female newborn presenting with intractable heart failure and respiratory distress soon after birth. Investigation by echocardiography showed severe persistent pulmonary hypertension of the newborn and patent ductus arteriosus. The hepatic angiogram revealed congenital hepatic arteriovenous malformation; therefore, secondary pulmonary artery hypertension complicated with 'steal' phenomenon was conclusively diagnosed.
引用
收藏
页码:673 / 675
页数:3
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